One of the significant problems in the modern world is the detection of improvised explosives made of materials synthesized at home. Such compounds include triacetone triperoxide (TATP) and hexamethylene triperoxide diamine (HMTD). An attempt was made to construct an instrument allowing for the simultaneous detection of both compounds despite the large difference of vapor pressure: very high for TATP and very low for HMTD. The developed system uses differential ion mobility spectrometry (DMS) in combination with a specially designed gas sample injection system. The created system of detectors allowed for the detection of a high concentration of TATP and a very low concentration of HMTD. TATP detection was possible despite the presence of impurities—acetone remaining from the technological process and formed as a coproduct of diacetone diperoxide (DADP) synthesis. Ammonia added to the carrier gas improved the possibility of detecting the abovementioned explosives, reducing the intensity of the acetone signal. The obtained results were then compared with the detection capabilities of drift tube ion mobility spectrometer (DT-IMS), which has not made possible such detection as DMS.

Detecting trace amounts of explosives is important for maintaining national security due to the growing threat of terror attacks. Particularly challenging is the increasing use of homemade explosives. Therefore, there is a constant need to improve existing technologies for detecting trace amounts of explosives. This paper describes the design of a stationary device (a gate) for detecting trace amounts of explosives and explosive taggants and the design of differential ion mobility spectrometers with a focus on the gas system. Nitromethane (NM), trimeric acetone peroxide (TATP), hexamine peroxide (HMTD), and explosive taggants 2,3-dimethyl-2,3-dinitrobutane (DMDNB) and 4-nitrotoluene (4NT) were used in this study. Gate measurements were carried out by taking air from the hands, pocket area, and shoes of the tested person. Two differential ion mobility spectrometers operating in two different modes were used as explosive detectors: a mode with a semi-permeable membrane to detect explosives with high vapor pressures (such as TATP) and a mode without a semi-permeable membrane (using direct introduction of the sample into the measuring chamber) to detect explosives with low vapor pressures (such as HMTD). The device was able to detect trace amounts of selected explosives/explosive taggants in 5 s.

The article presents a technique of differential ion mobility spectrometry (DMS) applicable to the detection and identification of volatile organic compounds (VOCs) from such categories as n-alkanes, alcohols, acetate esters, ketones, botulinum toxin, BTX, and fluoro- and chloro-organic compounds. A possibility of mixture identification using only the DMS spectrometer is analyzed, and several examples are published for the first time. An analysis of different compounds and their mechanisms of fragmentation, influence on effective ion temperature, and high electric field intensity is discussed.

DMS Technology is based on ion segregation phenomenon when flowing through the volume of the detector. DMS detector is made up with two parallel ceramic plates with electrodes layered on each plate. High voltage and high frequency of electric field generated in detector’s volume causes ion segregation on collection electrode (see Fig. 1). Fig. 1

Diagram of DMS detector composition.

Observed ion segregation in flowing gas is caused by different mobilities of the analyzed chemicals in fields characterized by lower and higher intensity. Ion mobility value is dependent on ion mass, charge and velocity of flowing gas [1–4]. Figure 2 depicts example flow gas through detector’s volume. Variable electric field put on electrodes causes capturing of these ions, which mobility does not enable stable (parallel to detector’s plates) flow through detector’s volume. Thus, phenomenon of ion mobility of ions flowing through the detector variable on compensated electrical field, makes detector a

It has become increasingly important to monitor environment contamination by such chemicals as chemical warfare agents (CWAs) and industrial toxic chemicals (TICs), as well as radiation hazards around and inside collective protection facilities. This is especially important given the increased risk of terrorist or military attacks. The Military Institute of Chemistry and Radiometry (MICR) has constructed and developed the ALERT device for the effective monitoring of these threats. This device uses sensors that detect chemical and radiological contaminations in the air. The CWA detector is an ion mobility spectrometer, TICs are detected by electrochemical sensors, and radiation hazards are detected via Geiger–Muller tubes. The system was designed to protect the crew from contamination. When chemical or radioactive contamination is detected at the air inlet for the shelter, air filtration through a carbon filter is activated. At this time, the air test procedure at the filter outlet is started to test the condition of the filter on an ongoing basis. After detecting contamination at the filter outlet, the system turns off the air pumping and the service can start the procedure of replacing the damaged carbon filter. This paper presents the results of laboratory testing of the ALERT gas alarm detector, which showed high measurements for important parameters, including sensitivity, repeatability, accuracy, and speed.

This paper deals with the problem of detecting benzyl methyl ketone (BMK), which is a precursor of amphetamine that can be synthesized in home labs. The focus of our work was to identify an improvement for the analysis of sewage introduced into the municipal sewage system. The sensors used to detect BKM in these systems are often clogged and therefore cannot function properly. In this article, a new method of detecting BMK and other chemicals in wastewater is presented. A system containing capillary polypropylene, hydrophobized with polysiloxane coating fibers was prepared. These solutions were used for continuous online measurements by ion mobility spectrometry. The use of pipes with a polysiloxane coating reduces the permeation of water and significantly increases the BMK permeation due to its high solubility in the polymer.